SEROTONIN- serotonin (hydrochloride) liquid
Deseret Biologicals, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

DRUG FACTS:

ACTIVE INGREDIENTS:

Serotonin 6X, 12x, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS:

For temporary relief of sleep disorders, joint pain, mood swings, depression, obsessive/compulsive behavior, lethargy, Seasonal Affective Disorder, itching and poor appetite.

WARNINGS:

Keep out of reach ofchildren. In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, contact a Poison Control Center right away.

DIRECTIONS:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

For temporary relief of sleep disorders, joint pain, mood swings, depression, obsessive/compulsive behavior, lethargy, Seasonal Affective Disorder, itching and poor appetite.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicials, Inc.

469 Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE DISPLAY LABEL:

DESBIO

NDC 43742-0295-1

HOMEOPATHIC

SEROTONIN

1 FL OZ (30 ml)

Serotonin

SEROTONIN
serotonin (hydrochloride) liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0295
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SEROTONIN HYDROCHLORIDE (UNII: GKN429M9VS) (SEROTONIN - UNII:333DO1RDJY)	SEROTONIN	6 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-0295-1	30 mL in 1 BOTTLE, DROPPER; Type 1: Convenience Kit of Co-Package	09/30/2013	08/05/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/30/2013	08/05/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0295) , api manufacture(43742-0295) , label(43742-0295) , pack(43742-0295)

Revised: 11/2018

Document Id: ffd927ef-dca2-497b-b051-e7b994435672

Set id: 6ce12a4c-67cb-4972-94bb-03934c152449

Version: 2

Effective Time: 20181107

Deseret Biologicals, Inc.